EP1245204B1 - Knee prosthesis - Google Patents

Knee prosthesis Download PDF

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Publication number
EP1245204B1
EP1245204B1 EP01811196A EP01811196A EP1245204B1 EP 1245204 B1 EP1245204 B1 EP 1245204B1 EP 01811196 A EP01811196 A EP 01811196A EP 01811196 A EP01811196 A EP 01811196A EP 1245204 B1 EP1245204 B1 EP 1245204B1
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EP
European Patent Office
Prior art keywords
angle
knee prosthesis
accordance
condyle
contact surfaces
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP01811196A
Other languages
German (de)
French (fr)
Other versions
EP1245204A3 (en
EP1245204A2 (en
Inventor
Vincent Leclercq
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zimmer GmbH
Original Assignee
Zimmer GmbH
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Filing date
Publication date
Application filed by Zimmer GmbH filed Critical Zimmer GmbH
Priority to EP01811196A priority Critical patent/EP1245204B1/en
Publication of EP1245204A2 publication Critical patent/EP1245204A2/en
Publication of EP1245204A3 publication Critical patent/EP1245204A3/en
Application granted granted Critical
Publication of EP1245204B1 publication Critical patent/EP1245204B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/38Joints for elbows or knees
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/38Joints for elbows or knees
    • A61F2/3859Femoral components
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • AHUMAN NECESSITIES
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    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30433Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements using additional screws, bolts, dowels, rivets or washers e.g. connecting screws
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30476Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements locked by an additional locking mechanism
    • A61F2002/30492Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements locked by an additional locking mechanism using a locking pin
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    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30535Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30604Special structural features of bone or joint prostheses not otherwise provided for modular
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    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30667Features concerning an interaction with the environment or a particular use of the prosthesis
    • A61F2002/30688Means for allowing passage or sliding of tendons or ligaments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30772Apertures or holes, e.g. of circular cross section
    • A61F2002/30777Oblong apertures
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30795Blind bores, e.g. of circular cross-section
    • A61F2002/30805Recesses of comparatively large area with respect to their low depth
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/3082Grooves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30878Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
    • A61F2002/30891Plurality of protrusions
    • A61F2002/30892Plurality of protrusions parallel
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30904Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves serrated profile, i.e. saw-toothed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/46Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
    • A61F2002/4631Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor the prosthesis being specially adapted for being cemented
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • AHUMAN NECESSITIES
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    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
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    • A61F2220/0025Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2220/0041Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements using additional screws, bolts, dowels or rivets, e.g. connecting screws
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    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00389The prosthesis being coated or covered with a particular material
    • A61F2310/00952Coating, pre-coating or prosthesis-covering structure made of bone cement, e.g. pre-applied PMMA cement mantle

Definitions

  • the invention relates to a knee prosthesis with a femoral component, which has guide surfaces for a patella and at least one condyle, which outer contact surfaces at an acute angle ⁇ ⁇ 90 ° and which along a straight line in the pivoting range of the angle ⁇ with contact surfaces on resection surfaces on the stump Femurbochens is pushed on.
  • Document FR-A-2768329 discloses the features of the preamble of claim 1.
  • the condyles in the form of an upwardly open "U" on a pre-machined femur bone and secure.
  • the femoral stump in the area of the natural condyles is brought to the shape of the contact surfaces of the artificial condylar parts, in order subsequently to fix them.
  • the attachment itself can be made by projecting pins on the contact surfaces, by wedging the outer, opposing contact surfaces and / or by fixing the contact surfaces with bone cement.
  • the condyles rest on a meniscal component or on a platform and can be pivoted on their running surfaces by a flexion angle ⁇ during the articulation of the knee joint relative to the platform or to the tibia.
  • the upper half of the prosthesis has guide surfaces for an anterior patella, and during flexion, the patella, which is offset by about 90 ° from the platform, slides on its own guide surfaces on the upper half of the prosthesis.
  • the support surfaces of the upper half of the prosthesis form a "U" -shaped opening towards the top, in the extension the patella on the front leg and the platform abut the bottom of this "U", while in flexion the bottom under the patella and the rear leg to Platform turns. Both forces from the patella from the front and forces from behind occur on the femoral stump when flexed from the platform, which are intercepted by opposing, approximately mutually perpendicular resection surfaces.
  • the associated outer contact surfaces are at a small angle to each other, so that when pushed by the wedge effect a tight fit is achieved to the denture stump.
  • the flexion angle achievable with such a prosthesis is insufficient because they are inherently accustomed to living at a greater flexion angle and bring a knee prosthesis into flexion angles for which the latter are not suitable.
  • the femoral component has a central part with guide surfaces for the patella and a condyle part separately slidable thereon which has outer abutment surfaces at an acute angle ⁇ ⁇ 90 ° and which along a straight line in the swivel range of the angle ⁇ on resection surfaces at the stump of the femur is pushed.
  • the object of the invention is to show construction forms that allow large angles of flexion in an open joint. This object is achieved in that the center line of the angle ⁇ is pivoted on the condyle part with respect to the center line of the angle ⁇ at the central part by an angle 15 ° ⁇ ⁇ ⁇ 60 ° to allow greater flexion.
  • the advantage of the invention is that even with great flexion, the forces that are transmitted through the prosthesis shell on the prosthesis stump are compressive forces. There are no shear loads between contact surfaces and resection surfaces, which are opposite to the Aufschieberaum. Due to the fact that the upper part of the prosthesis is in a central part and is divided into a condyle part, the parting line extends so that the guide surfaces for the patella are arranged in the middle part and treads to the platform on the condyle part are arranged, these surfaces can be made independently and pushed independently in mutually pivoted Aufschieichtung on the femoral stump become. Despite different Aufschieregache can contact surfaces of the middle part and the condyle share together on a Resetechnischsthesis.
  • the Aufschieregonne are, for example, by an angle ⁇ between 15 ° and 60 ° pivoted to allow a large flexion angle ⁇ . In this case, flexion angles ⁇ of more than 120 °, for example 160 °, are possible.
  • the condyles may be connected to a yoke or carried out individually. In the deferred state, the condyles are aligned through the resection surfaces, ie via the femoral stump to the middle part.
  • midsection and condyle parts may be movably guided in sagittal planes to provide similar patellar and platform force application points to the femur stump as in a natural knee joint. But it is also possible to connect the middle part and condyle by a coupling member in the pushed state.
  • individual contact surfaces may have pockets to bring a minimum amount of bone cement.
  • Individual contact surfaces in particular the outer contact surfaces, can have a toothed anchoring structure for a primary anchoring.
  • individual pins which extend in Aufschiebeiques and are provided for in the direction of insertion holes, improve the primary anchorage.
  • the non-bone cement-wetted contact surfaces may be coated with a coating that promotes bone growth.
  • Bearing surfaces which are wetted by bone cement may be coated with a bonding agent.
  • a coating may for example be composed of a Titanalalkoholat and an alkoxysilane.
  • the engaged radius of curvature of the condyles may continuously or sharply decrease to interfere with increasing flexion to allow lateral deflection of the condyles.
  • the figures show femoral parts of knee prostheses which have a central part 2 and a condyle part 3 with abutment surfaces 4a, 5a, 6a, 6b, 7b, 8a, 9a, 10a, 11a, 11b, 12a, 12b, 13b to form a resected femoral stump 1 ,
  • the middle part 2 has guide surfaces 20 for a patella 19 and outer contact surfaces 4a, 5a which are at an acute angle ⁇ ⁇ 90 ° to each other, while the condyle part 3 running surfaces 27, 28 for the articulation movement and outer abutment surfaces 6b, 7b at an acute angle ⁇ ⁇ 90 ° to each other.
  • Middle part 2 and condyle part 3 are separately on the femur stump in mutually pivoted Aufsteckraumen attachable to allow greater flexion, wherein the center line of the angle ⁇ relative to the center line of the angle ⁇ by an angle 15 ° ⁇ ⁇ ⁇ 60 ° is pivoted.
  • resection surfaces 4, 6, 11, 12, 12, 13, 7 and in the region between the condyles resection surfaces 4, 8, 9, 10, 5 are attached to a femoral stump 1 in the region of the condyles.
  • the resection surfaces 4 and 5 as well as the outer abutment surfaces 4a, 5a of the middle part 2 adjoining them are almost parallel to one another at an acute angle.
  • the middle part is supported by the contact surfaces 8a, 9a, 10a between the condyles and with further contact surfaces 6a, 11a, 12a on resection surfaces in the region of the former natural condyles, these resection surfaces also occupied by contact surfaces 6b, 11b, 12b of the condyle part 3 to center in the trench between the condyles and to provide support for the patellar guide surfaces 20 even with complete flexion.
  • the middle part is attachable from below along the center line 15 of the angle ⁇ , while the Aufsteckides and the center line 16 of the angle ⁇ is pivoted by an angle ⁇ of 45 ° to even at a larger flexion angle ⁇ , for example ⁇ > 120 °, an outer bearing surface 7b, in which the contact force presses the surface 7b into the stump or at most perpendicular to the surface 7b.
  • the running surface 27 of the condyle part 3 and the running surface 18 of a meniscus part 18 have the same radius of curvature R 1 .
  • FIG. 4 Another example is shown in Figures 4, 5, 6, 7, 8, 9.
  • the middle part 2 has abutment surfaces 4a, 6a, 8a, 11a, 5a and lateral centering surfaces 31.
  • the condyle part 2 has a yoke 14 which connects the actual condyles.
  • a parting line 25 between the middle part 2 and the condyle part 3 is laid (FIGS. 8, 9) so that the guide surfaces 20 for the patella 19 and the running surfaces 27, 28 of the condyles are not interrupted.
  • a recess 24 is provided for cruciate ligaments.
  • a portion of the abutment surfaces 4a, 6a, 8a, 11a has pockets 17, which are filled with bone cement when pushed on to allow a minimum layer thickness of bone cement in certain areas.
  • the pockets 17 and abutment surfaces may also be pre-cemented with a primer and a thin layer of bone cement.
  • Middle part 2 and condyle part 3 have holes 22, so that they can be connected to a femoral stub with a coupling piece in the form of a pin 32 after plugging. Due to this composite, the femoral stump is trapped at the same time because it is enclosed by contact surfaces at a wrap angle of more than 180 °.
  • the detail of the abutment surface 4a shows that in the case of outer abutment surfaces which face each other at a very acute angle, such as in FIG. 6, the surfaces 4a and 5a, it may be expedient to provide this surface with a toothing which has a tooth surface good primary anchorage allows and secures the middle part 2 until the condyle part 3 is attached.

Abstract

A femur portion has center guide surfaces (20) for patella and a condyle (3) that can be pushed on separately. The femur portion has contact surface (6a) at an acute angle beta ( beta ) that can be pushed onto the resection area (7) at the stump of femur bone in the pivot range of the angle beta. The condyle center line is pivoted through angle about 15-60 degrees to allow greater flexion.

Description

Die Erfindung handelt von einer Knieprothese mit einem Femurteil, welcher Führungsflächen für eine Patella und mindestens eine Kondyle aufweist, welcher äussere Anlageflächen in einem spitzen Winkel α ≤ 90° besitzt und welcher entlang einer Geraden im Schwenkbereich des Winkels α mit Anlageflächen auf Resektionsflächen am Stumpf eines Femurknochens aufschiebbar ist. Dokument FR-A-2768329 offenbart die Merkmale des Oberbegriffs von Anspruch 1.The invention relates to a knee prosthesis with a femoral component, which has guide surfaces for a patella and at least one condyle, which outer contact surfaces at an acute angle α ≤ 90 ° and which along a straight line in the pivoting range of the angle α with contact surfaces on resection surfaces on the stump Femurbochens is pushed on. Document FR-A-2768329 discloses the features of the preamble of claim 1.

Bisher ist es üblich, bei einer Knieprothese die Kondylen in Form eines nach oben geöffneten "U" auf einen vorbearbeiteten Femurknochen aufzuschieben und zu befestigen. Dazu wird der Femurstumpf im Bereich der natürlichen Kondylen auf die Form der Anlageflächen der künstlichen Kondylenteile gebracht, um diese anschliessend zu befestigen. Die Befestigung selbst kann durch vorstehende Zapfen an den Anlageflächen, durch ein Verkeilen der äusseren, sich gegenüberliegenden Anlageflächen und / oder durch ein Fixieren der Anlageflächen mit Knochenzement vorgenommen werden. Die Kondylen liegen auf einem Meniskusteil oder auf einer Plattform auf und können während der Artikulation des Kniegelenkes relativ zur Plattform respektive zur Tibia auf ihren Laufflächen um einen Flexionswinkel δ geschwenkt werden.So far, it is customary in a knee prosthesis delay the condyles in the form of an upwardly open "U" on a pre-machined femur bone and secure. For this purpose, the femoral stump in the area of the natural condyles is brought to the shape of the contact surfaces of the artificial condylar parts, in order subsequently to fix them. The attachment itself can be made by projecting pins on the contact surfaces, by wedging the outer, opposing contact surfaces and / or by fixing the contact surfaces with bone cement. The condyles rest on a meniscal component or on a platform and can be pivoted on their running surfaces by a flexion angle δ during the articulation of the knee joint relative to the platform or to the tibia.

In der EP-A-0 519 873 sind künstliche Kniegelenke gezeigt, bei denen je nach dem Zustand der Bänder auch eine mehr oder weniger wirksame seitliche Führung der Kondylen während der Artikulation möglich ist.In EP-A-0 519 873 artificial knee joints are shown in which, depending on the condition of the ligaments, more or less effective lateral guidance of the condyles during articulation is possible.

Die obere Prothesenhälfte besitzt Führungsflächen für eine Patella, die gegen anterior angeordnet ist und während der Flexion gleitet die Patella, welche um etwa 90° zur Plattform versetzt ist, auf eigenen Führungsflächen an der oberen Prothesenhälfte. Die Auflageflächen der oberen Prothesenhälfte bilden eine "U"-förmige Öffnung gegen oben, wobei in der Extension die Patella am vorderen Schenkel und die Plattform am Boden dieses "U" anliegen, während bei der Flexion der Boden unter die Patella und der hintere Schenkel zur Plattform dreht. Am Femurstumpf treten sowohl Kräfte von der Patella von vorn als auch Kräfte von hinten bei Flexion von der Plattform auf, die durch gegenüberliegende, annähernd zueinander senkrecht stehende Resektionsflächen abgefangen werden. Bei den meisten oberen Prothesenteilen stehen die zugehörigen äusseren Anlageflächen in einem kleinen Winkel zueinander, damit beim Aufschieben durch die Keilwirkung ein fester Sitz zum Prothesenstumpf erreicht wird. Für viele Bewohner im asiatischen Raum ist der mit einer solchen Prothese erreichbare Flexionswinkel ungenügend, da sie von Natur aus mit einem grösseren Flexionswinkel zu leben gewohnt sind und eine Knieprothese in Flexionswinkel bringen, für die letztere nicht geeignet sind.The upper half of the prosthesis has guide surfaces for an anterior patella, and during flexion, the patella, which is offset by about 90 ° from the platform, slides on its own guide surfaces on the upper half of the prosthesis. The support surfaces of the upper half of the prosthesis form a "U" -shaped opening towards the top, in the extension the patella on the front leg and the platform abut the bottom of this "U", while in flexion the bottom under the patella and the rear leg to Platform turns. Both forces from the patella from the front and forces from behind occur on the femoral stump when flexed from the platform, which are intercepted by opposing, approximately mutually perpendicular resection surfaces. In most upper prosthesis parts, the associated outer contact surfaces are at a small angle to each other, so that when pushed by the wedge effect a tight fit is achieved to the denture stump. For many Asian residents, the flexion angle achievable with such a prosthesis is insufficient because they are inherently accustomed to living at a greater flexion angle and bring a knee prosthesis into flexion angles for which the latter are not suitable.

Im FR-A-2768329 weist der Femurteil ein Mittelteil mit Führungsflächen für die Patella und ein davon getrennt aufschiebbares Kondylenteil auf, welches äussere Anlageflächen in einem spitzen Winkel β ≤ 90° besitzt und welches entlang einer Geraden im Schwenkbereich des Winkels β auf Resektionsflächen am Stumpf des Femurknochens aufschiebbar ist. Aufgabe der Erfindung ist es, Konstruktionsformen aufzuzeigen, die bei einem offenen Gelenk grosse Flexionswinkel ermöglichen. Diese Aufgabe wird dadurch gelöst, dass die Mittellinie des Winkels β am Kondylenteil gegenüber der Mittellinie des Winkels α am Mittelteil um einen Winkel 15° ≤ γ ≤ 60° verschwenkt ist, um eine grössere Flexion zu ermöglichen.In FR-A-2768329, the femoral component has a central part with guide surfaces for the patella and a condyle part separately slidable thereon which has outer abutment surfaces at an acute angle β ≤ 90 ° and which along a straight line in the swivel range of the angle β on resection surfaces at the stump of the femur is pushed. The object of the invention is to show construction forms that allow large angles of flexion in an open joint. This object is achieved in that the center line of the angle β is pivoted on the condyle part with respect to the center line of the angle α at the central part by an angle 15 ° ≤ γ ≤ 60 ° to allow greater flexion.

Der Vorteil der Erfindung liegt darin, dass auch bei grosser Flexion die Kräfte, welche durch das Prothesenoberteil auf den Prothesenstumpf übertragen werden, Druckkräfte sind. Es treten keine Scherbelastungen zwischen Anlageflächen und Resektionsflächen auf, die entgegen der Aufschieberichtung sind. Dadurch, dass der Prothesenoberteil in ein Mittelteil und in ein Kondylenteil aufgeteilt ist, deren Trennfuge so verläuft, dass die Führungsflächen für die Patella im Mittelteil angeordnet sind und Laufflächen zur Plattform auf dem Kondylenteil angeordnet sind, können diese Flächen unabhängig voneinander gefertigt werden und unabhängig voneinander in zueinander verschwenkten Aufschieberichtungen auf den Femurstumpf aufgeschoben werden. Trotz unterschiedlicher Aufschieberichtungen können Anlageflächen von Mittelteil und von Kondylenteil gemeinsam an einer Resektionsfläche anliegen. Die Aufschieberichtungen sind beispielsweise um einen Winkel γ zwischen 15° und 60° verschwenkt, um einen grossen Flexionswinkel δ zu ermöglichen. Dabei sind Flexionswinkel δ von mehr als 120° beispielsweise 160° möglich. Die Kondylen können mit einem Joch verbunden sein oder einzeln ausgeführt sein. Im aufgeschobenen Zustand sind die Kondylen durch die Resektionsflächen, d. h. über den Femurstumpf zum Mittelteil ausgerichtet. Zusätzlich können Mittelteil und Kondylenteile in sagittalen Ebenen zueinander beweglich geführt sein, um am Femurstumpf ähnliche Kraftangriffspunkte von Patella und Plattform wie bei einem natürlichen Kniegelenk zu erhalten. Es besteht aber auch die Möglichkeit Mittelteil und Kondylen durch ein Kupplungsorgan im aufgeschobenen Zustand zu verbinden.The advantage of the invention is that even with great flexion, the forces that are transmitted through the prosthesis shell on the prosthesis stump are compressive forces. There are no shear loads between contact surfaces and resection surfaces, which are opposite to the Aufschieberichtung. Due to the fact that the upper part of the prosthesis is in a central part and is divided into a condyle part, the parting line extends so that the guide surfaces for the patella are arranged in the middle part and treads to the platform on the condyle part are arranged, these surfaces can be made independently and pushed independently in mutually pivoted Aufschieichtung on the femoral stump become. Despite different Aufschieregungen can contact surfaces of the middle part and the condyle share together on a Resektionsfläche. The Aufschieregungen are, for example, by an angle γ between 15 ° and 60 ° pivoted to allow a large flexion angle δ. In this case, flexion angles δ of more than 120 °, for example 160 °, are possible. The condyles may be connected to a yoke or carried out individually. In the deferred state, the condyles are aligned through the resection surfaces, ie via the femoral stump to the middle part. In addition, midsection and condyle parts may be movably guided in sagittal planes to provide similar patellar and platform force application points to the femur stump as in a natural knee joint. But it is also possible to connect the middle part and condyle by a coupling member in the pushed state.

Für eine Befestigung mit Knochenzement können einzelne Anlageflächen Taschen aufweisen um eine Mindestmenge an Knochenzement einzubringen. Einzelne Anlageflächen insbesondere die äusseren Anlageflächen können eine gezahnte Verankerungsstruktur für eine Primärverankerung aufweisen. Ebenso können einzelne Zapfen, die in Aufschieberichtung verlaufen und für die in Aufschieberichtung Bohrungen vorgesehen sind, die Primärverankerung verbessern. Die nicht mit Knochenzement benetzten Anlageflächen können mit einem Belag beschichtet sein, der das Knochenwachstum fördert.For attachment with bone cement individual contact surfaces may have pockets to bring a minimum amount of bone cement. Individual contact surfaces, in particular the outer contact surfaces, can have a toothed anchoring structure for a primary anchoring. Likewise, individual pins which extend in Aufschieberichtung and are provided for in the direction of insertion holes, improve the primary anchorage. The non-bone cement-wetted contact surfaces may be coated with a coating that promotes bone growth.

Anlageflächen, die von Knochenzement benetzt werden, können mit einem Haftvermittler beschichtet sein. So ein Belag kann beispielsweise aus einem Titanalalkoholat und einem Alkoxysilan aufgebaut sein.Bearing surfaces which are wetted by bone cement may be coated with a bonding agent. Such a coating may for example be composed of a Titanalalkoholat and an alkoxysilane.

Während der Flexion kann sich der im Eingriff stehende Krümmungsradius der Kondylen kontinuierlich oder sprungweise verringern, um mit zunehmender Flexion eine seitliche Auslenkung der Kondylen zu ermöglichen.During flexion, the engaged radius of curvature of the condyles may continuously or sharply decrease to interfere with increasing flexion to allow lateral deflection of the condyles.

Im folgenden wird die Erfindung anhand von Ausführungsbeispielen beschrieben. Es zeigen:

Fig. 1:
schematisch einen Femurstumpf mit vorbearbeiteten Resektionsflächen, auf den ein gemäss
Fig. 2:
schematisch gezeigtes Mittelteil entlang einer Mittellinie aufschiebbar ist und ein gemäss
Fig. 3:
schematisch gezeigtes Kondylenteil entlang einer um einen Winkel γ verschwenkten Mittellinie aufschiebbar ist;
Fig. 4:
schematisch eine Ansicht für ein weiteres Beispiel von einem Mittelteil;
Fig. 5:
schematisch ein zu Figur 4 passendes Kondylenteil mit einem Joch;
Fig. 6:
schematisch eine Seitenansicht von Figur 4;
Fig. 7:
schematisch eine Seitenansicht von Figur 5;
Fig. 8:
schematisch eine Ansicht von unten der Figuren 4 und 5 vor dem Aufschieben
Fig. 9:
schematisch Mittelteil und Kondylenteil von Figur 8 nach dem Aufschieben
Fig. 10:
schematisch eine Ansicht von einem Mittelteil mit zwei voneinander unabhängigen Kondylen vor dem Aufschieben;
Fig. 11:
schematisch unter einem etwas anderen Blickwinkel die Teile von Figur 10 nach dem Aufschieben; und
Fig. 12:
schematisch einen vergrösserten Ausschnitt einer äusseren Anlagefläche mit einer Zahnung für die Primärverankerung.
In the following the invention will be described by means of embodiments. Show it:
Fig. 1:
schematically a Femurstumpf with pre-machined resection surfaces on the one according
Fig. 2:
schematically shown middle part along a center line can be pushed and a according to
3:
schematically shown condyle part can be pushed along a center line pivoted by an angle γ;
4:
schematically a view of another example of a central part;
Fig. 5:
schematically a matching to Figure 4 condyle part with a yoke;
Fig. 6:
schematically a side view of Figure 4;
Fig. 7:
schematically a side view of Figure 5;
Fig. 8:
schematically a bottom view of Figures 4 and 5 before pushing
Fig. 9:
schematically middle part and condyle part of Figure 8 after pushing
Fig. 10:
schematically a view of a central part with two independent condyles before pushing on;
Fig. 11:
schematically from a slightly different angle, the parts of Figure 10 after sliding; and
Fig. 12:
schematically an enlarged section of an outer contact surface with a toothing for the primary anchorage.

In den Figuren sind Femurteile von Knieprothesen gezeigt, die ein Mittelteil 2 und ein Kondylenteil 3 mit Anlageflächen 4a, 5a, 6a, 6b, 7b, 8a, 9a, 10a, 11a, 11b, 12a, 12b, 13b zu einem reserzierten Femurstumpf 1 besitzen. Dabei besitzt der Mittelteil 2 Führungsflächen 20 für eine Patella 19 und äussere Anlageflächen 4a, 5a die in einem spitzen Winkel α ≤ 90° zueinander stehen, während der Kondylenteil 3 Laufflächen 27, 28 für die Artikulationsbewegung und äussere Anlageflächen 6b, 7b in einem spitzen Winkel β ≤ 90° zueinander besitzt. Mittelteil 2 und Kondylenteil 3 sind getrennt voneinander auf den Femurstumpf in zueinander verschwenkten Aufsteckrichtungen aufsteckbar um eine grössere Flexion zu ermöglichen, wobei die Mittellinie des Winkels β gegenüber der Mittellinie des Winkels α um einen Winkel 15° ≤ γ ≤ 60° verschwenkt ist.The figures show femoral parts of knee prostheses which have a central part 2 and a condyle part 3 with abutment surfaces 4a, 5a, 6a, 6b, 7b, 8a, 9a, 10a, 11a, 11b, 12a, 12b, 13b to form a resected femoral stump 1 , In this case, the middle part 2 has guide surfaces 20 for a patella 19 and outer contact surfaces 4a, 5a which are at an acute angle α ≤ 90 ° to each other, while the condyle part 3 running surfaces 27, 28 for the articulation movement and outer abutment surfaces 6b, 7b at an acute angle β ≤ 90 ° to each other. Middle part 2 and condyle part 3 are separately on the femur stump in mutually pivoted Aufsteckrichtungen attachable to allow greater flexion, wherein the center line of the angle β relative to the center line of the angle α by an angle 15 ° ≤ γ ≤ 60 ° is pivoted.

Im folgenden sind für gleiche Funktionen gleiche Hinweiszeichen verwendet.In the following the same signs are used for the same functions.

Im Beispiel der Figuren 1,2 und 3 sind an einem Femurstumpf 1 im Bereich der Kondylen Resektionsflächen 4, 6, 11, 12, 12, 13, 7 und im Bereich zwischen den Kondylen Resektionsfiächen 4, 8, 9, 10, 5 angebracht. Die Resektionsflächen 4 und 5 sowie die daran anliegenden äusseren Anlageflächen 4a, 5a des Mittelteils 2 stehen in einem spitzen Winkel fast parallel zueinander. Das Mittelteil stützt sich mit den Anlageflächen 8a, 9a, 10a zwischen den Kondylen und mit weiteren Anlageflächen 6a, 11a, 12a auf Resektionsflächen im Bereich der früheren, natürlichen Kondylen ab, wobei diese Resektionsflächen auch von Anlageflächen 6b, 11b, 12b des Kondylenteils 3 belegt werden, um eine Zentrierung im Graben zwischen den Kondylen vorzunehmen und um den Führungsflächen 20 für die Patella 19 auch bei vollständiger Flexion Unterstützung zu geben.In the example of FIGS. 1, 2 and 3, resection surfaces 4, 6, 11, 12, 12, 13, 7 and in the region between the condyles resection surfaces 4, 8, 9, 10, 5 are attached to a femoral stump 1 in the region of the condyles. The resection surfaces 4 and 5 as well as the outer abutment surfaces 4a, 5a of the middle part 2 adjoining them are almost parallel to one another at an acute angle. The middle part is supported by the contact surfaces 8a, 9a, 10a between the condyles and with further contact surfaces 6a, 11a, 12a on resection surfaces in the region of the former natural condyles, these resection surfaces also occupied by contact surfaces 6b, 11b, 12b of the condyle part 3 to center in the trench between the condyles and to provide support for the patellar guide surfaces 20 even with complete flexion.

Der Mittelteil ist entlang der Mittellinie 15 des Winkels α von unten aufsteckbar, während die Aufsteckrichtung und die Mittellinie 16 des Winkels β um einen Winkel γ von 45° verschwenkt ist um auch bei einem grösseren Flexionswinkel δ, beispielsweise δ > 120°, eine äussere Anlagefläche 7b zu schaffen, bei der die Kontaktkraft die Fläche 7b in den Stumpf hinein oder höchstens senkrecht zur Fläche 7b presst. Wie aus Figur 3 ersichtlich ist, haben die Lauffläche 27 des Kondylenteils 3 und die Lauffläche 18 eines Meniskusteils 18 den gleichen Krümmungsradius R1.The middle part is attachable from below along the center line 15 of the angle α, while the Aufsteckrichtung and the center line 16 of the angle β is pivoted by an angle γ of 45 ° to even at a larger flexion angle δ, for example δ> 120 °, an outer bearing surface 7b, in which the contact force presses the surface 7b into the stump or at most perpendicular to the surface 7b. As can be seen from FIG. 3, the running surface 27 of the condyle part 3 and the running surface 18 of a meniscus part 18 have the same radius of curvature R 1 .

Ein weiteres Beispiel ist in den Figuren 4, 5, 6, 7, 8, 9 gezeigt. Auch hier müssen wegen des vergrösserten Flexionswinkels die Führungsflächen 20 für die Patella 19 und die Laufflächen 27, 28 in Flexionsrichtung verlängert werden. Der Mittelteil 2 besitzt Anlageflächen 4a, 6a, 8a, 11a, 5a und seitliche Zentrierflächen 31. Der Kondylenteil 2 besitzt ein Joch 14 welches die eigentlichen Kondylen verbindet. Eine Trennfuge 25 zwischen dem Mittelteil 2 und dem Kondylenteil 3 ist so gelegt (Fig. 8, 9), dass die Führungsflächen 20 für die Patella 19 und die Laufflächen 27, 28 der Kondylen nicht unterbrochen sind. Eine Aussparung 24 ist für Kreuzbänder vorgesehen. Ein Teil der Anlageflächen 4a, 6a, 8a, 11a besitzt Taschen 17, die beim Aufschieben mit Knochenzement gefüllt werden, um eine Mindestschichtdicke an Knochenzement in bestimmten Bereichen zu ermöglichen. Die Taschen 17 und Anlageflächen können auch mit einem Haftvermittler und einer dünnen Schicht aus Knochenzement vorzementiert sein.Another example is shown in Figures 4, 5, 6, 7, 8, 9. Again, because of the increased flexion angle, the guide surfaces 20 for the patella 19 and the treads 27, 28 are extended in the direction of flexion. The middle part 2 has abutment surfaces 4a, 6a, 8a, 11a, 5a and lateral centering surfaces 31. The condyle part 2 has a yoke 14 which connects the actual condyles. A parting line 25 between the middle part 2 and the condyle part 3 is laid (FIGS. 8, 9) so that the guide surfaces 20 for the patella 19 and the running surfaces 27, 28 of the condyles are not interrupted. A recess 24 is provided for cruciate ligaments. A portion of the abutment surfaces 4a, 6a, 8a, 11a has pockets 17, which are filled with bone cement when pushed on to allow a minimum layer thickness of bone cement in certain areas. The pockets 17 and abutment surfaces may also be pre-cemented with a primer and a thin layer of bone cement.

Gemäss dem spitzen Winkel α in Figur 6 muss das Aufschieben des Mittelteils 2 in etwa in der Richtung der Mittellinie 15 erfolgen, während beim Kondylenteil mit einem weniger spitzen Winkel β eine grössere Abweichung der Aufschieberichtung von der Mittellinie des Winkels β möglich ist. Hier wird die Aufschieberichtung, die innerhalb des Winkels β liegen muss, durch die Richtung der Zapfen 23 bestimmt. In Figur 5 und 7 ist eine Erzeugende für die Kontur der Kondylenlaufflächen 27, 28 angedeutet. Der Krümmungsradius R1 der Laufflächen 27, 28 geht mit zunehmender Flexion in einen kleineren Krümmungsradius R2 über.According to the acute angle .alpha. In FIG. 6, the center part 2 must be slid open approximately in the direction of the center line 15, whereas in the case of the condyle part with a less acute angle .beta. A greater deviation of the pushing direction from the center line of the angle .beta. Is possible. Here, the Aufschieberichtung, which must be within the angle β, determined by the direction of the pins 23. In FIGS. 5 and 7, a generatrix for the contour of the condyle running surfaces 27, 28 is indicated. The radius of curvature R 1 of the running surfaces 27, 28 merges with increasing flexion into a smaller radius of curvature R 2 .

Mittelteil 2 und Kondylenteil 3 besitzen Bohrungen 22, damit sie nach dem Aufstecken auf den Femurstumpf mit einem Kupplungsstück in Form eines Stiftes 32 verbunden werden können. Durch diesen Verbund ist der Femurstumpf gleichzeitig gefangen, da er auf einem Umschlingungswinkel von mehr als 180° von Anlageflächen umschlossen ist.Middle part 2 and condyle part 3 have holes 22, so that they can be connected to a femoral stub with a coupling piece in the form of a pin 32 after plugging. Due to this composite, the femoral stump is trapped at the same time because it is enclosed by contact surfaces at a wrap angle of more than 180 °.

In Figur 12 zeigt der Ausschnitt der Anlagefläche 4a, dass es im Fall von äusseren Anlageflächen, die in einem sehr spitzen Winkel wie beispielsweise in Figur 6 die Flächen 4a und 5a zueinanderstehen, sinnvoll sein kann, diese Fläche mit einer Zahnung zu versehen, die eine gute Primärverankerung ermöglicht und den Mittelteil 2 sichert, bis auch der Kondylenteil 3 aufgesteckt ist.In FIG. 12, the detail of the abutment surface 4a shows that in the case of outer abutment surfaces which face each other at a very acute angle, such as in FIG. 6, the surfaces 4a and 5a, it may be expedient to provide this surface with a toothing which has a tooth surface good primary anchorage allows and secures the middle part 2 until the condyle part 3 is attached.

Am Beispiel der Figuren 10 und 11 ist eine Anordnung gezeigt, bei der zwei separate Kondylenteile 3 mit Laufflächen 27, 28 aufsteckbar sind und über Bohrungen 22 durch ein Kupplungsstück, beispielsweise einen Stift oder eine Schraube, mit dem Mittelteil 2 verbunden werden können. Wenn es der Bandapparat am Knie erlaubt, können diese beiden Kondylenteile 3 auch von der Seite her eingebracht werden, da sie nicht fest mit einem Joch verbunden sind, um dann - je nachdem wie lang die Zapfen 23 gestaltet sind - in der Aufschieberichtung der Zapfen ihre Verankerung zu finden. Sobald ein Kondylenteil 3 mit dem Mittelteil 2 verbunden ist, wird auch hier der Femurstumpf auf einem Umschlingungswinkel von mehr als 180° umschlossen und ist ohne Risiko ein Flexionswinkel von mehr als 120° möglich.The example of Figures 10 and 11, an arrangement is shown in which two separate condyle parts 3 with treads 27, 28 are attachable and can be connected via holes 22 by a coupling piece, such as a pin or a screw with the middle part 2. If the ligaments on the knee allowed, these two condyle parts 3 can also be introduced from the side, since they are not firmly connected to a yoke, then - depending on how long the pins 23 are designed - in the direction of the pins their To find anchoring. As soon as a condyle part 3 is connected to the middle part 2, the femur stump is enclosed here at an angle of wrap of more than 180 ° and, without risk, a flexion angle of more than 120 ° is possible.

Claims (14)

  1. A knee prosthesis having a femur part which has guide surfaces (20) for a patella (19) and at least one condyle (18), which has outer contact surfaces (4a, 5a) at an acute angle α ≤ 90° and whose contact surfaces can be pushed onto resection areas (4, 5, 6, 8, 9, 10, 11, 12) at the stump of a femur bone (1) along a straight line in the pivot range of the angle α, wherein the femur part has a centre part (2) with guide surfaces (20) for the patella (19) and a condyle part (3) which can be pushed on separately therefrom, which has outer contact surfaces (6b, 7b) at an acute angle β ≤ 90° and which can be pushed onto resection areas (6, 7, 11, 12, 13) at the stump of the femur bone along a straight line in the pivot range of the angle β, characterised in that the centre line (16) of the angle β at the condyle part (3) is pivoted through an angle of 15° ≤ γ ≤ 60° with respect to the centre line (15) of the angle α at the centre part (2) in order to allow a greater flexion.
  2. A knee prosthesis in accordance with claim 1, characterised in that the condyle part (3) has a flexion angle δ of more than 120°.
  3. A knee prosthesis in accordance with claim 1 or claim 2, characterised in that the condyle part (3) has two condyles (3) each outwardly disposed with respect to the centre part (2) which are connected via a yoke (14).
  4. A knee prosthesis in accordance with any of claims 1 to 3, characterised in that the centre part (2) and the condyle part (3) are connectable to one another by a coupling member (21) in the pushed-on state.
  5. A knee prosthesis in accordance with claim 4, characterised in that the coupling member (21) consists of a pin inserted transversely through separating surfaces or of a transversely throughgoing screw connection.
  6. A knee prosthesis in accordance with any one of claims 1 to 5, characterised in that the angle γ is between 40° and 50°.
  7. A knee prosthesis in accordance with any of claims 1 to 6, characterised in that individual contact surfaces (4a, 5a, 6a, 6b, 7b, 8a, 9a, 10a, 11a, 11b, 12a, 12b, 13b) have pockets (17) in order to introduce a minimum quantity of bone cement for a fastening with bone cement.
  8. A knee prosthesis in accordance with any one of claims 1 to 6, characterised in that individual contact surfaces (4a, 5a, 6a, 6b, 7b, 8a, 9a, 10a, 11a, 11b, 12a, 12b, 13b) have a serrated anchoring structure (30) for a primary anchoring.
  9. A knee prosthesis in accordance with any of claims 1 to 6, characterised in that individual contact surfaces (4a, 5a, 6a, 6b, 7b, 8a, 9a, 10a, 11a, 11b, 12a, 12b, 13b) are covered with a coating which promotes bone growth or enhances the adhesion of bone cement.
  10. A knee prosthesis in accordance with claim 9, characterised in that the film contains substances such as hydroxyl appatite or is made up of a titanal alcoholate and an alkoxy silane.
  11. A knee prosthesis in accordance with any of claims 1 to 10, characterised in that the radius of curvature R1 of the condyles (3) is reduced at least once in the contact region from the transition of the extension to the full flexion.
  12. A knee prosthesis in accordance with any of claims 1 to 11, characterised in that the angle α or β is less than 10°.
  13. A knee prosthesis in accordance with any of claims 1 to 11, characterised in that the angle α or β is less than 5°.
  14. A knee prosthesis in accordance with any of claims 1 to 13, characterised in that spigots (23) are attached to contact surfaces (12b) in the direction of pushing on which facilitate centering and primary anchoring.
EP01811196A 2001-03-26 2001-12-07 Knee prosthesis Expired - Lifetime EP1245204B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP01811196A EP1245204B1 (en) 2001-03-26 2001-12-07 Knee prosthesis

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP01810301 2001-03-26
EP01810301 2001-03-26
EP01811196A EP1245204B1 (en) 2001-03-26 2001-12-07 Knee prosthesis

Publications (3)

Publication Number Publication Date
EP1245204A2 EP1245204A2 (en) 2002-10-02
EP1245204A3 EP1245204A3 (en) 2004-01-14
EP1245204B1 true EP1245204B1 (en) 2007-02-07

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Family Applications (1)

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EP01811196A Expired - Lifetime EP1245204B1 (en) 2001-03-26 2001-12-07 Knee prosthesis

Country Status (8)

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US (1) US20020138150A1 (en)
EP (1) EP1245204B1 (en)
JP (1) JP3738221B2 (en)
KR (1) KR100628446B1 (en)
CN (1) CN1236738C (en)
AT (1) ATE353200T1 (en)
DE (1) DE50112004D1 (en)
ES (1) ES2278716T3 (en)

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Also Published As

Publication number Publication date
US20020138150A1 (en) 2002-09-26
JP3738221B2 (en) 2006-01-25
DE50112004D1 (en) 2007-03-22
JP2002291779A (en) 2002-10-08
KR20020076112A (en) 2002-10-09
CN1376450A (en) 2002-10-30
ES2278716T3 (en) 2007-08-16
ATE353200T1 (en) 2007-02-15
EP1245204A3 (en) 2004-01-14
EP1245204A2 (en) 2002-10-02
KR100628446B1 (en) 2006-09-26
CN1236738C (en) 2006-01-18

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